Development of a whole-cell biosensor for β-lactamase inhibitor discovery

被引:2
|
作者
Jeffs, Mitchell A. [1 ]
Gray, Rachel A. V. [1 ]
Sheth, Prameet M. [1 ,2 ]
Lohans, Christopher T. [1 ]
机构
[1] Queens Univ, Dept Biomed & Mol Sci, Kingston, ON, Canada
[2] Queens Univ, Dept Pathol & Mol Med, Kingston, ON, Canada
关键词
IN-VITRO ACTIVITY; PSEUDOMONAS-AERUGINOSA; CARBAPENEMASE; NXL104; AMPR; COMBINATIONS; CEFTAZIDIME; RESISTANCE;
D O I
10.1039/d3cc03583b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The production of beta-lactamases by bacterial pathogens endangers antimicrobial therapy, and new inhibitors for beta-lactamases are urgently needed. We report the development of a luminescent-based biosensor that quantifies beta-lactamase inhibition in a cellular context, based on the activation of transcriptional factor AmpR following the exposure of bacterial cells to beta-lactams. This rapid method can account for factors like membrane permeability and can be employed to identify new beta-lactamase inhibitors. We developed a whole-cell biosensor that quantifies beta-lactamase inhibition in a cellular context. This assay accounts for factors such as membrane permeability and can be used to identify novel beta-lactamase inhibitors.
引用
收藏
页码:12707 / 12710
页数:4
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